Wilkes S R, Trautmann J C, DeSanto L W, Campbell R J
Mayo Clin Proc. 1979 Apr;54(4):258-60.
A 16-year-old white boy presented with a history of amaurosis fugax associated with an afferent pupillary defect, proptosis, discomfort of the left eye. Tomograms of the skull and of the orbit revealed a lobulated 4-cm ivory osteoma arising from the left ethmoid sinus and extending into the maxillary sinus and left orbit. After surgical extirpation, visual acuity returned to normal and the papilledema resolved after 4 months. This patient is 1 of 37 patients with osteoma of the paranasal sinuses or of the orbit (or of both) who underwent surgical treatment at the Mayo Clinic between the years 1948 and 1977. Twelve of these patients had orbital involvement, and only these patients had ocular signs and symptoms.
一名16岁白人男孩，有发作性黑矇病史，伴有传入性瞳孔障碍、眼球突出及左眼不适。头颅和眼眶断层照片显示，一个分叶状的4厘米象牙样骨瘤，起源于左侧筛窦，延伸至上颌窦和左侧眼眶。手术切除后，视力恢复正常，4个月后视乳头水肿消退。该患者是1948年至1977年间在梅奥诊所接受手术治疗的37例鼻窦或眼眶（或两者皆有）骨瘤患者之一。其中12例患者眼眶受累，只有这些患者有眼部体征和症状。
